Ensure compliance with GCP, SOPs, protocols, and regulatory standards Financial & Contract ... Support CRA and team training on therapeutic areas and study-specific needs * Foster collaboration ...
Ensure compliance with GCP, SOPs, protocols, and regulatory standards Financial & Contract ... Support CRA and team training on therapeutic areas and study-specific needs * Foster collaboration ...
Ensure compliance with GCP, SOPs, protocols, and regulatory standards Financial & Contract ... Support CRA and team training on therapeutic areas and study-specific needs * Foster collaboration ...
Ensure compliance with GCP, SOPs, protocols, and regulatory standards Financial & Contract ... Support CRA and team training on therapeutic areas and study-specific needs * Foster collaboration ...
Contract Cra information
See Indiana salary details
$11.44 - $16.43
0% of jobs
$16.43 - $21.42
8% of jobs
$21.42 - $26.41
13% of jobs
$27.75 is the 25th percentile. Wages below this are outliers.
$26.41 - $31.40
15% of jobs
$31.40 - $36.39
13% of jobs
The median wage is $37.14 / hr.
$36.39 - $41.38
11% of jobs
$41.38 - $46.37
12% of jobs
$48.14 is the 75th percentile. Wages above this are outliers.
$46.37 - $51.36
13% of jobs
$51.36 - $56.35
14% of jobs
$56.35 - $61.34
2% of jobs
$61.34 - $66.34
1% of jobs
$11
$39
$66
How much do contract cra jobs pay per hour?
As of Jul 18, 2026, the average hourly pay for contract cra in Indiana is $39.13, according to ZipRecruiter salary data. Most workers in this role earn between $27.45 and $50.10 per hour, depending on experience, location, and employer.
What are some common challenges faced by Contract Clinical Research Associates (CRAs) and how can they effectively manage them?
Contract CRAs often juggle multiple clinical trial sites and studies, which can make prioritizing and time management especially challenging. They must adapt quickly to each sponsor's protocols and systems, often with limited onboarding. Building strong relationships with site staff and maintaining clear, consistent communication are key to overcoming these challenges. Staying organized through meticulous documentation and leveraging digital tools can help contract CRAs efficiently meet monitoring visit deadlines and regulatory requirements.
What are the key skills and qualifications needed to thrive as a Contract CRA (Clinical Research Associate), and why are they important?
To thrive as a Contract CRA, you need a solid understanding of clinical research protocols, regulatory guidelines (like GCP/ICH), and typically a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and sometimes certifications like ACRP or SOCRA are beneficial. Strong attention to detail, excellent organizational skills, and effective communication are crucial soft skills for managing multiple studies and collaborating with sites. These competencies are essential for ensuring compliance, data integrity, and the smooth execution of clinical trials.
What Are Contract CRA Jobs?
A contract clinical research associate (contract CRA) is a temporary position in which you manage clinical trials and scientific research projects. As a contractor, you work temporarily on a contract that typically lasts for the duration of the project. Clinical research associates work in the pharmaceutical industry to ensure the safety and effectiveness of medication or vaccines. You can also work on studies for biotech companies and projects that perform analysis on surgical procedures or treatments. Your duties focus on planning the trial, defining the parameters, ensuring the safety of participants, and making sure the project meets all regulations and requirements.
What are contract crafters?
Contract crafters are professionals who specialize in creating, reviewing, and negotiating contracts for individuals or organizations. They ensure that agreements are legally sound, clearly written, and protect the interests of all parties involved. Contract crafters may work in a variety of industries, including business, law, real estate, and technology. Their expertise helps minimize risk and ensure compliance with relevant laws and regulations.
More about Contract Cra jobs
What are the most commonly searched types of Cra jobs in Indiana? The most popular types of Cra jobs in Indiana are:
What are popular job titles related to Contract Cra jobs in Indiana? For Contract Cra jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Contract Cra jobs in Indiana look for? The top searched job categories for Contract Cra jobs in Indiana are:
- Remote Clinical Research Phlebotomist
- Remote Clinical Research Coverage Analyst
- Clinical Research Regulatory Assistant
- Remote Airline Dietitian
- Clinical Research Associate Remote
- Temporary Visa Sponsorship Clinical Research
- Centralized Monitor Clinical Research
- Associate Etmf
- Junior Clinical Research Associate
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What cities in Indiana are hiring for Contract Cra jobs? Cities in Indiana with the most Contract Cra job openings:
IQVIA rating
8.1
Based on 53 frontline employees who took The Breakroom Quiz
55th of 210 rated it services
Job description
IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.
Drive global clinical trials from first site activation to final patient visit-own the strategy, accelerate delivery, and shape the future of clinical research worldwide.
Required Experience
Job Overview- 2+ years of global study management experience
- Experience across multiple countries/regions
- Phase I-III clinical trials experience (Phase III required)
- Oncology experience required
- Ability to work across multiple therapeutic areas
We are seeking a Global Study Manager responsible for the end-to-end planning, execution, and delivery of clinical trial site management activities across global studies. This role ensures successful site selection, activation, monitoring oversight, and closeout-while balancing speed, quality, and cost. You will serve as the primary point of contact for clients, lead cross-functional teams, and ensure compliance with ICH-GCP, regulatory requirements, and study protocols. This is a highly visible role that combines strategic leadership, operational execution, and financial oversight.
Key ResponsibilitiesGlobal Study & Site Leadership- Lead site management strategy from study award through close-out
- Oversee site identification, selection, activation, and recruitment performance
- Ensure clinical monitoring processes meet study needs and timelines
- Partner with CRAs to optimize enrollment, data quality, and compliance
- Serve as primary client contact and own key customer relationships
- Lead cross-functional teams across regions and cultures
- Facilitate internal and external meetings, including executive presentations
- Drive collaboration across stakeholders, vendors, and functional leads
- Develop and manage integrated study plans and risk mitigation strategies
- Proactively identify risks and implement corrective/preventative actions
- Monitor study timelines, enrollment trends, and data quality metrics
- Ensure compliance with GCP, SOPs, protocols, and regulatory standards
- Manage study financials, including forecasting and revenue acceleration
- Identify and manage out-of-scope work and change orders
- Oversee Billing Unit Reviews (BURs) and expense approvals
- Track performance against budget and Estimate at Completion (EAC)
- Maintain TMF health and ensure timely document submission
- Develop quality monitoring plans and compliance metrics
- Ensure adherence to study tools, training materials, and processes
- Lead and mentor cross-functional project teams
- Support CRA and team training on therapeutic areas and study-specific needs
- Foster collaboration, knowledge sharing, and continuous improvement
- Bachelor's degree in life sciences or related field
- 5+ years of clinical research/monitoring experience, including 2 years in a clinical study management role
- Strong knowledge of ICH-GCP, FDA regulations, and clinical trial processes
- Experience managing global clinical trials and multi-regional teams
- Demonstrated experience in project financial management
- Exceptional communication and stakeholder management skills
- Strong problem-solving and risk mitigation capabilities
- Ability to influence without authority in matrix organizations
- High attention to detail and quality-driven mindset
- Proficiency in Microsoft Office and clinical systems (e.g., CTMS, EDC)
- Work on cutting-edge global trials across therapeutic areas
- Collaborate with top talent in a dynamic, global environment
- Make a direct impact on patient outcomes worldwide
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $93,100.00 - $232,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
About IQVIA
Sourced by ZipRecruiter
At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.
Industry
Health care and social assistance
Company size
10,000+ Employees
Headquarters location
Durham, NC, US